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Showing results (131-140 of 136) with videos related to

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European Journal of Human Genetics : EJHG|August 14, 2014
Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utilityJia-Chi Wang, Leslie Ross, Loretta W Mahon, et al.
Clinical and Translational Science|December 17, 2013
Sildenafil increases muscle protein synthesis and reduces muscle fatigueMelinda Sheffield-Moore, John E Wiktorowicz, Kizhake V Soman, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
Investigation of NRXN1 deletions: clinical and molecular characterizationMindy Preston Dabell, Jill A Rosenfeld, Patricia Bader, et al.
Wellcome Open Research|June 15, 2018
The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with <i>de novo</i> constitutive <i>DNMT3A</i> variantsKatrina Tatton-Brown, Anna Zachariou, Chey Loveday, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 3, 2018
Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlationMagdalena Koczkowska, Tom Callens, Alicia Gomes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2018
Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlationMagdalena Koczkowska, Tom Callens, Alicia Gomes, et al.
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Showing results (131-140 of 136) with videos related to

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Pageof 14
You have reached the last page of results.This site can display upto 136 results.
European Journal of Human Genetics : EJHG|August 14, 2014
Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utilityJia-Chi Wang, Leslie Ross, Loretta W Mahon, et al.
Clinical and Translational Science|December 17, 2013
Sildenafil increases muscle protein synthesis and reduces muscle fatigueMelinda Sheffield-Moore, John E Wiktorowicz, Kizhake V Soman, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
Investigation of NRXN1 deletions: clinical and molecular characterizationMindy Preston Dabell, Jill A Rosenfeld, Patricia Bader, et al.
Wellcome Open Research|June 15, 2018
The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with <i>de novo</i> constitutive <i>DNMT3A</i> variantsKatrina Tatton-Brown, Anna Zachariou, Chey Loveday, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 3, 2018
Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlationMagdalena Koczkowska, Tom Callens, Alicia Gomes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2018
Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlationMagdalena Koczkowska, Tom Callens, Alicia Gomes, et al.
Pageof 14